| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:22516013-22516185 | Common:3; Rare:64 | ||||
| chr4:24584389-24584698 | Rare:101 | ||||
| chr4:25160546-25160728 | Common:1; Rare:50 | ||||
| chr4:25376984-25377331 | Common:3; Rare:104 | ||||
| chr4:25914016-25914308 | Common:3; Rare:128 | ||||
| chr4:26320450-26320860 | Common:1; Rare:139 | ||||
| chr4:26320874-26321045 | Rare:59; Clinvar (benign):1 | ||||
| chr4:26583981-26584124 | Rare:28 | ||||
| chr4:30719946-30720099 | Common:1; Rare:27 | ||||
| chr4:30720261-30720606 | Common:2; Rare:88 | ||||
| chr4:37826579-37826729 | Common:1; Rare:55 | ||||
| chr4:37977178-37977455 | Rare:66 | ||||
| chr4:38867588-38867826 | Common:2; Rare:84 | ||||
| chr4:39182220-39182538 | Rare:68; Clinvar:1 | ||||
| chr4:39366308-39366394 | Rare:24 |